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COL4A5 c.1390G>A
ALS1
DMD c.1332-11868C>G
TP53
肌萎缩侧索硬化症1型
USH2A c.8559-2A>G
囊性纤维化
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中文
罕见病
Microphthalmia, Syndromic 1 (MCOPS1)
Alias:
Lenz Microphthalmia Syndrome
Lenz Microphthalmia
Lenz Dysplasia
Mcops1
Microphthalmia, Syndromic 4
Syndromic Microphthalmia 1
Microphthalmia, Lenz Type
Microphthalmia or Anophthalmos with Associated Anomalies
Microphthalmia, Syndromic 4, Formerly
Microphthalmia, Syndromic, Type 1
Microphthalmia, Syndromic, 1
Syndromic Microphthalmia 4
Lenz Type Microphthalmia
Mcops4, Formerly
Anop1, Formerly
Maa, Formerly
Mcops4
Anop1
Maa
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基础信息
疾病表征
基因 & 突变
靶点药物
疾病模型
文献报道
小眼畸形,综合征1,也被称为Lenz小眼畸形综合征,与小眼畸形和小眼畸形,综合征2有关。与小眼畸形,综合征1有关的重要基因是NAA10(N-Alpha-Acetyltransferase 10,NatA催化亚基),其相关通路/超级通路包括代谢途径生物转化阶段I和II以及FBXL10增强弥漫性大B细胞淋巴瘤中的MAP/ERK信号通路。附属组织包括眼睛和皮肤,相关表型为小眼畸形和智力障碍。
Related ID:
MALACARDS:MCR263
OMIM:309800
MESH:D008850
Basic Information
Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
X染色体
X显
新生儿
--
23
120
15
MCR263
Medical Symptom
#
Categorization
Description
HPO Frequency
Orphanet Frequency
HPO Source Accession
No data available
Gene & Mutation
#
Gene
Function
Score
Mutations
No data available
Related Drugs
Name
CAS Number
Status
Phase
No data available
Disease Model
Category
Name
MGI
Related Gene
Strain of Origin
Publications
No data available
References Literature
Title
PMID
Journal
Year
IF
No Data Found!
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